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JAK2 V617F mutation analysis in different myeloid lineages (granulocytes, platelets, CFU-MK, BFU-E and CFU-GM) in essential thrombocythemia patients

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JAK2 V617F mutation analysis in different myeloid lineages (granulocytes, platelets, CFU-MK, BFU-E and CFU-GM) in essential thrombocythemia patients (English)

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L Florensa

1

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author name string

B Bellosillo

series ordinal

2

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C Besses

series ordinal

3

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E Puigdecanet

series ordinal

4

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B Espinet

series ordinal

5

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E Pérez-Vila

series ordinal

6

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R Longarón

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7

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R M Vilà

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8

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F Solé

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9

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S Serrano

series ordinal

10

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publication date

3 August 2006

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published in

Leukemia

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volume

20

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issue

10

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page(s)

1903-1905

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https://scigraph.springernature.com/pub.10.1038/sj.leu.2404341

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cites work

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

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https://api.crossref.org/works/10.1038%2FSJ.LEU.2404341

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21 January 2018

A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

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https://api.crossref.org/works/10.1038%2FSJ.LEU.2404341

retrieved

21 January 2018

A gain-of-function mutation of JAK2 in myeloproliferative disorders

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reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404341

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21 January 2018

Expression of a homodimeric type I cytokine receptor is required for JAK2V617F-mediated transformation

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reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404341

retrieved

21 January 2018

Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study.

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reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404341

retrieved

21 January 2018

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DOI

10.1038/SJ.LEU.2404341

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1038107712

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PubMed publication ID

16888614

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(Q58010180)

JAK2 V617F mutation analysis in different myeloid lineages (granulocytes, platelets, CFU-MK, BFU-E and CFU-GM) in essential thrombocythemia patients

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